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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BECTON, DICKINSON & CO. (SPARKS) BD MICROPROBE¿ PROCESSOR (120 V); STATION PIPETTING AND DILUTING, FOR CLINICAL USE

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BECTON, DICKINSON & CO. (SPARKS) BD MICROPROBE¿ PROCESSOR (120 V); STATION PIPETTING AND DILUTING, FOR CLINICAL USE Back to Search Results
Model Number 250100
Device Problem False Positive Result (1227)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 06/16/2021
Event Type  malfunction  
Manufacturer Narrative
Medical device expiration date: na.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
 
Event Description
It was reported that while using bd microprobe¿ processor (120 v) false positive results were obtained.Samples were retested on 2nd instrument and results were negative.There was no patient impact.The following information was provided by the initial reporter: false positives customer states they have a 2nd instrument and all specimen results were acceptable upon repeat.The instrument in question seems to be getting stuck on certain wells and does not wash the card using all the wells.
 
Event Description
It was reported that while using bd microprobe¿ processor (120 v) false positive results were obtained.Samples were retested on 2nd instrument and results were negative.There was no patient impact.The following information was provided by the initial reporter: false positives.Customer states they have a 2nd instrument and all specimen results were acceptable upon repeat.The instrument in question seems to be getting stuck on certain wells and does not wash the card using all the wells.
 
Manufacturer Narrative
H6: investigation summary: the complaint of "false positive" was reported against the affirm instrument catalog number 250100, serial number (b)(6).Customer reported that the instrument is not moving the pac card along all cassette wells and causing them all the beads to be blue.Customer was requested to remove the program card, clean it off with a kimwipe and use canned air in the card slot.Complaint was closed after three attempt to reach out to the customer.No parts were returned to bd for investigation.Root cause cannot be determined with the information provided.Complaint is confirmed.Investigation consisted of a review of the instrument installation, service history, and related complaint data.No new risks, trends, or hazards were identified.Bd will continually monitor for trend.H3 other text : see h10.
 
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Brand Name
BD MICROPROBE¿ PROCESSOR (120 V)
Type of Device
STATION PIPETTING AND DILUTING, FOR CLINICAL USE
Manufacturer (Section D)
BECTON, DICKINSON & CO. (SPARKS)
7 loveton circle
sparks MD 21152
Manufacturer (Section G)
BECTON, DICKINSON & CO. (SPARKS)
7 loveton circle
sparks MD 21152
Manufacturer Contact
katie swenson
9450 south state street
sandy, UT 84070
8015296192
MDR Report Key12163284
MDR Text Key263432628
Report Number1119779-2021-01158
Device Sequence Number1
Product Code JQW
UDI-Device Identifier00382902501008
UDI-Public00382902501008
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K923268
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Other,User Facility
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 01/20/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number250100
Device Catalogue Number250100
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 06/16/2021
Initial Date FDA Received07/13/2021
Supplement Dates Manufacturer Received01/20/2022
Supplement Dates FDA Received01/25/2022
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured11/11/2019
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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